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Genetic and biochemical study of dual hereditary jaundice: Dubin–Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2
Dual hereditary jaundice, a combination of Dubin–Johnson and Gilbert's syndromes, is a rare clinical entity resulting from the compound defects of bilirubin conjugation and transport. We aimed to study the hereditary jaundice in 56 members from seven seemingly unrelated Roma families, to find t...
Shranjeno v:
| izdano v: | Eur J Hum Genet |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Nature Publishing Group
2016
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4930088/ https://ncbi.nlm.nih.gov/pubmed/26350512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.181 |
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